Canonical Allele Identifier: CA137021948
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs545321609
gnomAD v3: 6-33004837-G-T
gnomAD v4: 6-33004837-G-T
MyVariant Identifiers: chr6:g.32972614G>T (hg19) chr6:g.33004837G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004837G>T , CM000668.2:g.33004837G>T GRCh38
NC_000006.11:g.32972614G>T , CM000668.1:g.32972614G>T GRCh37
NC_000006.10:g.33080592G>T NCBI36
NG_012007.1:g.9776C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2001C>A MANE Select ENSP00000229829.3:n.*2001C>A
ENST00000229829.6:c.*2001C>A ENSP00000229829.3:n.*2001C>A
NM_002119.3:c.*2001C>A NP_002110.1:n.*2001C>A
NM_002119.4:c.*2001C>A MANE Select NP_002110.1:n.*2001C>A
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